Canonical Allele Identifier: CA361048384

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974810C>A (hg19) ; chr5:g.137639121C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639121C>A , CM000667.2:g.137639121C>A	GRCh38
NC_000005.9:g.136974810C>A , CM000667.1:g.136974810C>A	GRCh37
NC_000005.8:g.137002709C>A	NCBI36
NG_032569.1:g.101970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1051G>T MANE Select	ENSP00000312397.4:p.Ala351Ser
ENST00000309755.8:c.1051G>T	ENSP00000312397.4:p.Ala351Ser
ENST00000502381.1:n.638G>T
ENST00000504208.5:c.*335-10684G>T	ENSP00000423585.1:n.*335-10684G>T
ENST00000505853.1:c.931G>T	ENSP00000426173.1:p.Ala311Ser
ENST00000506491.5:c.805G>T	ENSP00000424828.1:p.Ala269Ser
ENST00000506873.5:n.676G>T
ENST00000508657.5:c.955G>T	ENSP00000422099.1:p.Ala319Ser
NM_001257194.1:c.955G>T	NP_001244123.1:p.Ala319Ser
NM_001257195.1:c.805G>T	NP_001244124.1:p.Ala269Ser
NM_017415.2:c.1051G>T	NP_059111.2:p.Ala351Ser
NM_017415.3:c.1051G>T MANE Select	NP_059111.2:p.Ala351Ser
NM_001257195.2:c.805G>T	NP_001244124.1:p.Ala269Ser